TY - JOUR
T1 - Development of a biodegradable smooth-surface microcarrier for retinal pigment epithelial cell expansion and maturation
AU - Liu, Zengping
AU - Wong, Daniel Soo Lin
AU - Parikh, Bhav Harshad
AU - Li, Jian
AU - Al-Mubaarak, Abdurrahmaan
AU - Liu, Hang
AU - Yang, Binxia
AU - Bhargava, Mayuri
AU - Li, Zibiao
AU - Loh, Xian Jun
AU - Su, Xinyi
N1 - Publisher Copyright:
© 2025 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC license. http://creativecommons.org/licenses/by-nc/4.0/
PY - 2026/4
Y1 - 2026/4
N2 - The retinal pigment epithelium (RPE) is essential for the health and function of the retina and, more specifically, the photoreceptors. Hence, the dysfunction of RPE leads to various retinal degeneration diseases. The rising prevalence of these disorders highlights the need for effective, large-scale cell-based therapies, particularly those utilizing stem cell-derived RPE cells. This study presents the development of a biodegradable, smooth surface microcarrier designed to facilitate the expansion and maturation of RPE cells derived from induced pluripotent stem cells (iPSCs). Using a three-dimensional (3D) culture system with polycaprolactone (PCL) porous microcarriers, we demonstrate that RPE cells exhibit comparable adhesion and growth on microcarriers as they do on traditional two-dimensional (2D) culture plates. The microcarrier system facilitates efficient maturation and yields higher quantities of functional RPE cells, highlighting its potential for large-scale production to meet both clinical demands and in vitro large-scale screening studies. Moreover, RPE cells cultured on this microcarrier can be directly frozen and recovered, maintaining their phenotypic and functional integrity upon thawing. This research showcases the scalability and practicality of RPE cell production, providing a robust solution for the storage and delivery of RPE cells. While our results establish the feasibility of direct cryopreservation and recovery of monolayer RPE cells on microcarriers, the designation of a ‘ready-to-use’ product format is preliminary and will require expanded assessment of long-term functionality, safety, and direct translational outcomes in future studies.
AB - The retinal pigment epithelium (RPE) is essential for the health and function of the retina and, more specifically, the photoreceptors. Hence, the dysfunction of RPE leads to various retinal degeneration diseases. The rising prevalence of these disorders highlights the need for effective, large-scale cell-based therapies, particularly those utilizing stem cell-derived RPE cells. This study presents the development of a biodegradable, smooth surface microcarrier designed to facilitate the expansion and maturation of RPE cells derived from induced pluripotent stem cells (iPSCs). Using a three-dimensional (3D) culture system with polycaprolactone (PCL) porous microcarriers, we demonstrate that RPE cells exhibit comparable adhesion and growth on microcarriers as they do on traditional two-dimensional (2D) culture plates. The microcarrier system facilitates efficient maturation and yields higher quantities of functional RPE cells, highlighting its potential for large-scale production to meet both clinical demands and in vitro large-scale screening studies. Moreover, RPE cells cultured on this microcarrier can be directly frozen and recovered, maintaining their phenotypic and functional integrity upon thawing. This research showcases the scalability and practicality of RPE cell production, providing a robust solution for the storage and delivery of RPE cells. While our results establish the feasibility of direct cryopreservation and recovery of monolayer RPE cells on microcarriers, the designation of a ‘ready-to-use’ product format is preliminary and will require expanded assessment of long-term functionality, safety, and direct translational outcomes in future studies.
KW - Microcarriers
KW - Polycaprolactone
KW - Retinal pigment epithelium
KW - Stem cells
UR - https://www.scopus.com/pages/publications/105017725080
U2 - 10.1016/j.biomaterials.2025.123742
DO - 10.1016/j.biomaterials.2025.123742
M3 - Article
C2 - 41022012
AN - SCOPUS:105017725080
SN - 0142-9612
VL - 327
JO - Biomaterials
JF - Biomaterials
M1 - 123742
ER -